Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Krishna Hassomal Birjkumar"'
Autor:
Nicholas Phillips, Michael J. Kelly, Simon Aldridge, Cameron Jones, Krishna Hassomal Birjkumar, Jeffrey Harmer, Deepak Dange, Andrew D. Schwarz, Christina Y. Tang, Nikolas Kaltsoyannis, Philip Mountford, Rémi Tirfoin, Andrey V. Protchenko
Publikováno v:
Nature Chemistry. 6:315-319
The chemistry of the Group 13 metals is dominated by the +1 and +3 oxidation states, and simple monomeric M(II) species are typically short-lived, highly reactive species. Here we report the first thermally robust monomeric MX2 radicals of gallium, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ef7c93748e827cca40e41bcbc81181
https://doi.org/10.1038/nchem.1870
https://doi.org/10.1038/nchem.1870
Autor:
Cameron Jones, Andrew D. Schwarz, Andrey V. Protchenko, Simon Aldridge, Philip Mountford, Krishna Hassomal Birjkumar, Liban M. A. Saleh, Nikolas Kaltsoyannis
Reaction of [Ln(CH(2)SiMe(3))(2)(THF)(n)][BPh(4)] (Ln = Sc, Y, Lu ; n = 3, 4) with Li{B(NArCH)(2)}(THF)(2) (Ar = 2,6-C(6)H(3)(i)Pr(2)) formed the first group 3 and lanthanide boryl compounds, Sc{B(NArCH)(2)}(CH(2)SiMe(3))(2)(THF) and Ln{B(NArCH)(2)}(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::209df9398c3bd8b4113faa56a64d01a7
https://doi.org/10.1021/ja2007092
https://doi.org/10.1021/ja2007092
Autor:
Andrew D. Schwarz, Dragoslav Vidovic, Simon Aldridge, Cameron Jones, Nikolas Kaltsoyannis, Deepak Dange, Andrey V. Protchenko, Philip Mountford, Krishna Hassomal Birjkumar
Simple two-coordinate acyclic silylenes, SiR(2), have hitherto been identified only as transient intermediates or thermally labile species. By making use of the strong σ-donor properties and high steric loading of the B(NDippCH)(2) substituent (Dipp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c3af218bc2a0d12745c65b2fab213dd
https://doi.org/10.1021/ja301042u
https://doi.org/10.1021/ja301042u
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 41(18)
The geometries, relative energies and spectroscopic properties of a range of α-isosaccharinate complexes of uranyl(VI) are studied computationally using ground state and time-dependent density functional theory. The effect of pH is accommodated by v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c629343b41222c55ec886ff4927bf70f
https://pubmed.ncbi.nlm.nih.gov/22411275
https://pubmed.ncbi.nlm.nih.gov/22411275
Publikováno v:
MRS Proceedings. 1475
The geometries, relative energies and spectroscopic properties of α-isosaccharinate and D-gluconate complexes of uranyl(VI) are studied computationally using density functional theory. The effect of pH is accommodated by varying the number of water
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa79391ce82e6efc0121725616db8ef7
https://doi.org/10.1557/opl.2012.639
https://doi.org/10.1557/opl.2012.639
Publikováno v:
Dalton Transactions. 40:11248
The geometries, relative energies and spectroscopic properties of a range of D-gluconate complexes of uranyl(VI) are studied computationally using density functional theory. The effect of pH is accommodated by varying the number of water and hydroxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::870d2554089f0e077b20d184f402780e
https://doi.org/10.1039/c1dt11086a
https://doi.org/10.1039/c1dt11086a